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Merck
CN

D3292

Sigma-Aldrich

2,6-Di-tert-butylphenol

~99% (GC)

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About This Item

Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
128-39-2
Molecular Weight:
206.32
Beilstein:
1841887
EC Number:
204-884-0
MDL number:
MFCD00008820
UNSPSC Code:
12352200

Key Documents

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vapor pressure

<0.01 mmHg ( 20 °C)

Assay

~99% (GC)

bp

253 °C (lit.)

mp

34-37 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(C)(C)c1cccc(c1O)C(C)(C)C

InChI

1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3

InChI key

DKCPKDPYUFEZCP-UHFFFAOYSA-N

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Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

227.3 °F - closed cup

Flash Point(C)

108.5 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
071H3467
024H3557

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Ya-lei Zhang et al.
Journal of environmental sciences (China), 17(2), 271-275 (2005-11-22)
An aerobic bacterium strain, F-3-4, capable of effectively degrading 2, 6-ditert-butylphenol (2, 6-DTBP), was isolated and screened out from an acrylic fiber wastewater and the biofilm in the wastewater treatment facilities. This strain was identified as Alcaligenes sp. through morphological
J B Kramer et al.
Bioorganic & medicinal chemistry, 3(4), 403-410 (1995-04-01)
The preparation of hydroxylamine analogs of 2,6-di-tert-butylphenols (DTBP) and the inhibition of cyclooxygenase (CO) and 5-lipoxygenase (5-LO) by these compounds is discussed.
[Studies on the synthesis of anti-inflammatory activity of 2,6-di-tert-butylphenols with a heterocyclic group at the 4-position. IV. Photo-induced and base-catalyzed oxygenation of 4-(3,5-di-tert-butyl-4-hydroxyphenyl)-2-oxo-4-imidazolines].
Y Isomura et al.
Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan, 104(8), 909-914 (1984-08-01)
Y Fujimoto et al.
The Journal of pharmacy and pharmacology, 36(3), 195-197 (1984-03-01)
The inhibitory effects of NN'-diphenyl-p-phenylenediamine (DPPD), sodium diethyldithiocarbamate (SDDC) and 2,6-di-t-butylphenol (DTBP) on the generation of medullary prostaglandin E have been compared. DPPD (1 microM) and SDDC (1 mM) failed to inhibit arachidonic acid-induced stimulation of prostaglandin E synthesis, while
Shinsuke Ishihara et al.
Journal of the American Chemical Society, 133(40), 16119-16126 (2011-08-31)
Porphyrin derivatives bearing 2,6-di-tert-butylphenol substituents at their 5,15-positions undergo reversible photoredox switching between porphyrin and porphodimethene states as revealed by UV-vis spectroscopy, fluorescence spectroscopy, and X-ray single-crystal analyses. Photoredox interconversion is accompanied by substantial variations in electronic absorption and fluorescence
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